Endurance exercise combined with intermittent cold stimulation promoting white adipose tissue browning in rats

WANG Xiao LI Liang CUI Cheng-li CAI Zhi-ping YU Chang ZHANG Li-jia

Acta Anatomica Sinica ›› 2023, Vol. 54 ›› Issue (3) : 348-356.

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Acta Anatomica Sinica ›› 2023, Vol. 54 ›› Issue (3) : 348-356. DOI: 10.16098/j.issn.0529-1356.2023.03.014
Histology,Embryology and Developmental Biology

Endurance exercise combined with intermittent cold stimulation promoting white adipose tissue browning in rats

  • WANG  Xiao1  LI  Liang1*  CUI  Cheng-li1  CAI  Zhi-ping YU  Chang2  ZHANG  Li-jia2
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Abstract

Objective To explore the effect and mechanism of endurance exercise and intermittent cold stimulation on brown adipose tissue activity and white adipose tissue browning in obese rats.   Methods Totally 52 SD male obese rats were divided into normothermic control group (NC group),intermittent cold stimulation group (IC group),endurance exercise group (EE group) and endurance exercise combined with intermittent cold stimulation group (EI group),13 pieces per group. The ambient temperature of the normothermic control group was 24-26℃;The exercise group used animal running table exercise with a running speed of 20 m/min and a slope of 0°,50 minutes per exercise,exercise 2 times with 20 minutes interval; The cold stimulation group was exposed to an ambient temperature of 4℃ for 4 hours (in the cold storage), and stimulated 6 days per week for 4 weeks. After 4 weeks of continuous stimulation, positron emission tomography/computed tomography (PET/CT) was applied to detect the metabolism of interscapular brown adipose tissue (BAT) and browning of inguinal white adipose tissue (iWAT) in rats. Weighting,measuring body length,sampling tissue and collecting blood samples were detected the four lipids. The expression of mitochondrial uncoupling protein 1(UCP1),vascular endothelial growth factor-A(VEGF-A),p38 MAPK and peroxisome proliferator-activated receptor γ coactivator-1 (PGC-1α) in interscapular brown adipose tissue and inguinal white adipose tissue of rats were detected by immunohistochemistry and Western blotting.   Results The body weight,serum total cholesterol (CHOL),triglyceride(TG)and  low density lipoprotein (LDL)of IC,EE and EI groups decreased significantly. PET/CT showed that, in BAT,SUVmax increased significantly in IC,EE and EI groups;In iWAT,maximum standard intake value (SUVmax) increased significantly in EI group. Immunohistochemistry showed: in BAT and iWAT, the number and the density of adipocytes of IC, EE and EI groups increased,and iWAT adipocytes appeared brown adipocytes. Western blotting showed that, in the BAT, the expression level of UCP1 protein in IC,EE and EI groups increased significantly;In the iWAT, the expression levels of UCP1 and PGC-1α in IC group,EE group and EI group increased significantly ;The expression level of p38 MAPK protein in IC group and EI group increased significantly;The expression level of VEGF-A protein in EE group and EI group decreased significantly.  Conclusion All three experimental protocols can promote brown adipose tissue activation and white adipose tissue browning in obese rats after intervention,with intermittent cold stimulation combined with endurance exercise having the most significant effect.

Key words

Endurance exercise
/ Cold stimulation / White adipose tissue / Brown adipose tissue / Immunohistochemistry / Western blotting / Positron emission tomography/computedtomography / Rat 

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WANG Xiao LI Liang CUI Cheng-li CAI Zhi-ping YU Chang ZHANG Li-jia. Endurance exercise combined with intermittent cold stimulation promoting white adipose tissue browning in rats[J]. Acta Anatomica Sinica. 2023, 54(3): 348-356 https://doi.org/10.16098/j.issn.0529-1356.2023.03.014

References

[1]Harms M,Seale P. Brown and beige fat: development,function and therapeutic potential[J]. Nat Med,2013, 19(10):1252-1263.
[2]Bartelt A,Heeren J. Adipose tissue browning and metabolic health[J]. Nat Rev Endocrinol,2014, 10(1):24-36.
[3]Cao W,Daniel KW,Robidoux J,et al. p38 mitogen-activated protein kinase is the central regulator of cyclic AMP-dependent transcription of the brown fat uncoupling protein 1 gene[J]. Mol Cell Biol,2004, 24(7):3057-3067.
[4]Chen Y,Zhao M,Zheng T,et al. Repression of adipose vascular endothelial growth factor reduces obesity through adipose browning[J]. Am J Physiol Endocrinol Metab,2019, 316(2):E145-E155.
[5]Jing YL,Yang XZh,Bai ZhJ,et al. Effects of high-fat diet-induced obesity on ovarian function in female fertile rats[J]. Chinese Journal of Comparative Medicine,2019,29(8):106-110. (in Chinese)
景彦林,杨修昭,白振军,等.高脂饮食诱导肥胖对雌性生育大鼠卵巢功能的影响[J].中国比较医学杂志,2019,29(8):106-110.
[6]Zhu RX. Effect of aerobic exercise on the expression of ADRβ3-COX2-UCP1 in adipose tissue of rats on high-fat diet[D]. Beijing:Beijing University of Sports,2019.(in Chinese)
朱镕鑫. 有氧运动对高脂膳食大鼠脂肪组织ADRβ3-COX2-UCP1表达的影响[D]. 北京:北京体育大学,2019.
[7]Jebeile H, Kelly AS, O’Malley G, et al. Obesity in children and adolescents: epidemiology, causes, assessment and management [J]. Lancet Diabetes Endocrinol, 2020, 10(5):351365.
[8]Cannon B,Nedergaard J. Brown adipose tissue: function and physiological significance[J]. Physiol Rev,2004,84(1):277-359.
[9]Marlatt KL,Ravussin E. Brown adipose tissue: an update on recent findings[J]. Curr Obes Rep,2017,6(4):389-396.
[10]Nedergaard J,Golozoubova V,Matthias A,et al. UCP1: the only protein able to mediate adaptive non-shivering thermogenesis and metabolic inefficiency[J].Biochim Biophys Acta,2001,1504(1):82-106.
[11]Dewal RS,Stanford KI. Effects of exercise on brown and beige adipocytes[J]. Biochim Biophys Acta Mol Cell Biol Lipids,2019,1864(1):71-78.
[12]Lu X,Ji Y,Zhang L, et al. Resistance to obesity by repression of VEGF gene expression through induction of brown-like adipocyte differentiation[J].Endocrinology,2012,153(7):3123-3132.
[13]Jin H,Li D,Wang X,et al. VEGF and VEGFB play balancing roles in adipose differentiation,gene expression,and function[J]. Endocrinology,2018,159(5):2036-2049.
[14]Fischer K, Fenzl A, Liu D, et al. The scaffold protein p62 regulates adaptive thermogenesis through ATF2 nuclear target activation[J]. Nat Comman, 2020,11(1):2306.
[15]Matesanz N,Bernardo E,Acín-Pérez R,et al.MKK6 controls T3-mediated browning of white adipose tissue[J]. Nat Commun,2017,8(1):856.
[16]Sato S,Dyar KA,Treebak JT,et al. Atlas of exercise metabolism reveals time-dependent signatures of metabolic homeostasis[J].Cell Metab,2022,34(2):329-345.e8.
[17]Bedford TG,Tipton CM,Wilson NC,et al. Maximum oxygen consumption of rats and its changes with various experimental procedures[J].J Appl Physiol Respir Environ Exerc Physiol,1979,47(6):1278-1283.
[18]Yao L,Cui X,Chen Q,et al. Cold-inducible SIRT6 regulates thermogenesis of brown and beige fat[J].Cell Rep,2017,20(3):641-654.
[19]Paschos GK,Tang SY,Theken KN,et al. Cold-induced browning of inguinal white adipose tissue is independent of adipose tissue cyclooxygenase-2[J].Cell Rep,2018,24(4):809-814.
[20]Finlin BS,Zhu B,Confides AL,et al. Mast cells promote seasonal white adipose beiging in humans[J].Diabetes,2017,66(5):1237-1246.
[21]Kern PA,Finlin BS,Zhu B,et al. The effects of temperature and seasons on subcutaneous white adipose tissue in humans: evidence for thermogenic gene induction[J].J Clin Endocrinol Metab,2014,99(12):E2772-E2779.
[22]van der Lans AA,Hoeks J,Brans B,et al. Cold acclimation recruits human brown fat and increases nonshivering thermogenesisJ].J Clin Invest,2013,123(8):3395-3403.
[23]Stanford KI, Lynes MD,Takahashi H, et al. 12,13-diHOME: an exercise-induced lipokine that increases skeletal muscle fatty acid uptake[J].Cell Metab,2018,27(5):1111-1120.e3.
[24]Thirupathi A, da Silva Pieri BL, Queiroz JAMP, et al. Strength training and aerobic exericse alter mitochondrial parameters in brow adipose tissue and equally reduce body adiposity in aged rats[J]. J Physiol Biochem, 2019, 75(1):101-108.
[25]Xu X,Ying Z,Cai M,et al. Exercise ameliorates high-fat diet-induced metabolic and vascular dysfunction, and increases adipocyte progenitor cell population in brown adipose tissue[J].Am J Physiol Regul Integr Comp Physiol,2011,300(5):R1115-R1125.
[26]Wu MV,Bikopoulos G,Hung S,et al. Thermogenic capacity is antagonistically regulated in classical brown and white subcutaneous fat depots by high fat diet and endurance training in rats: impact on whole-body energy expenditure[J].J Biol Chem,2014,289(49):34129-34140.
[27]Vosselman MJ,Hoeks J,Brans B,et al. Low brown adipose tissue activity in endurance-trained compared with lean sedentary men[J].Int J Obes (Lond),2015,39(12):1696-1702.
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